2-[2-Methyl-1-(2-methylphenyl)propylidene]propanedinitrile

Base Information

Chemical Name:2-[2-Methyl-1-(2-methylphenyl)propylidene]propanedinitrile
CAS No.:73700-28-4
Molecular Formula:C₁₄H₁₄N₂
Molecular Weight:210.279
Hs Code.:
DSSTox Substance ID:DTXSID101194748

Synonyms:2-[2-Methyl-1-(2-methylphenyl)propylidene]propanedinitrile;DTXSID101194748;73700-28-4

Suppliers and Price of 2-[2-Methyl-1-(2-methylphenyl)propylidene]propanedinitrile

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-[2-Methyl-1-(2-methylphenyl)propylidene]propanedinitrile

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:210.115698455
Heavy Atom Count:16
Complexity:354

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=CC=C1C(=C(C#N)C#N)C(C)C

Technology Process of 2-[2-Methyl-1-(2-methylphenyl)propylidene]propanedinitrile

There total 1 articles about 2-[2-Methyl-1-(2-methylphenyl)propylidene]propanedinitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 529-19-1
2-Methylbenzonitrile

: 1068-55-9
isopropylmagnesium chloride

: 109-77-3
malononitrile

: 73700-28-4
2-methyl-1-(o-tolyl)-propylidenemalononitrile

Guidance literature:: Yield given. Multistep reaction; 1.) toluene, 16 h, reflux, 2.) ether;

Reference yield:

: 73700-28-4
2-methyl-1-(o-tolyl)-propylidenemalononitrile

: 2-(o-bromomethylphenyl)-2-isopropoxy-3,3-dimethyl-1,1-cyclopropanedicarbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 13 percent / N-bromosuccinimide, bis(1-cyano-1-methylethyl)diazene / CCl₄ / 15 h / Heating; Irradiation

2: propan-2-ol / 0.5 h / Ambient temperature

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; isopropyl alcohol;

Reference yield:

: 73700-28-4
2-methyl-1-(o-tolyl)-propylidenemalononitrile

: 3,3-dimethyl-2-o-tolyl-1,1-cyclopropanedicarbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 13 percent / N-bromosuccinimide, bis(1-cyano-1-methylethyl)diazene / CCl₄ / 15 h / Heating; Irradiation

2: 35 percent / sodium borohydride / ethanol / 20 h / Ambient temperature

With sodium tetrahydroborate; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; ethanol;